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At least 91 records · Page 5Linked to original sources
USGS1981

Sequential extraction techniques applied to a porphyry copper deposit in the basin and range province

Samples of minus-80-mesh (<180 μm) stream sediment, rock containing exposed fracture coatings, and jarosite and chrysocolla were collected from an area surrounding the North Silver Bell porphyry Cu deposit near Tucson, Arizona. The samples were subjected to a series of extractions in a scheme originally designed for use on samples from humid or sub-humid environments, in which the following fractions can effectively be separated: (1) carbonates and exchangeable metals; (2) Mn oxides; (3) organic compounds and sulfides; (4) hydrous Fe oxides; and (5) residual crystalline minerals. Jarosite and chrysocolla, two major minerals of the North Silver Bell area, were found to dissolve over two or more steps of the extraction scheme. The results represent only a limited number of samples from one copper deposit. Nevertheless, they do suggest that in a semiarid to arid environment, where mechanical dispersion of such minerals predominates, uncritical assignment of unique phases, such as Mn oxides or organics to a given extraction would lead to false interpretations of weathering processes. However, the relative proportions of elements dissolved in each step of the jarosite and chrysocolla extractions could be used as a “fingerprint” for recognition of the presence of these two minerals in the stream-sediment and rock samples. The relative abundance of hydrous Fe oxide and jarosite and the alteration zoning could be mapped using data from jarosite and chrysocolla extractions. Manganese oxides were also found to have a greater influence on Zn than on Cu or Pb during supergene alteration. The rapid change in relative importance of the first (1 M -acetic acid) extraction for Cu, Zn, and Pb near the mineralized zone suggested the occurrence of minor hydromorphic processes within the stream sediments. Thus, the acetic acid extraction proved the most effective for pinpointing mineralization in sediments. In contrast, the residual fraction had the longest dispersion train, suggesting that total metal concentrations are most effective in arid environments for reconnaissance surveys.

Journal of Geochemical Exploration↗
USGS1982

Uranium in spring water and bryophytes at basin creek in central idaho

Arkosic sandstones and conglomerates of Tertiary age beneath the Challis Volcanics of Eocene age at Basin Creek, 10 km northeast of Stanley, Idaho, contain uranium-bearing vitrainized carbon fragments. The economic potential of these sandstones and conglomerates is currently being assessed. Springs abound at the contacts of rock units, and water from these springs supports abundant growths of bryophytes (mosses and liverworts). Water from 22 springs and associated bryophytes were sampled; two springs were found to contain apparently anomalous concentrations (normalized) of uranium — as much as 6.5 μg/L (ppb) in water and 1800 μg/g (ppm) in ash of mosses. Moss samples from both springs also contained anomalous concentrations of arsenic, and one contained highly anomalous amounts of beryllium. Water from a third spring contained slightly anomalous amounts of uranium, and two species of mosses at the spring contained anomalous uranium (400 and 700 μg/g) and high levels of both cadmium and lead. Water from a fourth spring was normal for uranium (0.18 μg/L), but the moss from the water contained a moderate uranium level and highly anomalous concentrations of lead, germanium, and thallium. These results suggest that, in the Basin Creek area, moss sampling at springs may give a more reliable indication of uranium occurrence than would water sampling. The reason for this may be the ability of mosses to concentrate uranium and its associated pathfinder elements and to integrate uranium fluctuations that occur in the spring water over any period of time.

Idaho↗
USGS1982

Uraniferous opal, Virgin Valley, Nevada: Conditions of formation and implications for uranium exploration

Uraniferous, fluorescent opal, which occurs in tuffaceous sedimentary rocks at Virgin Valley, Nevada, records the temperature and composition of uranium-rich solutions as well as the time of uranium-silica coprecipitation. Results are integrated with previous geologic and geochronologic data for the area to produce a model for uranium mobility that may be used to explore for uranium deposits in similar geologic settings. Uraniferous opal occurs as replacements of diatomite, or silicic air-fall ash layers in tuffaceous lakebeds of the Virgin Valley Formation (Miocene) of Merriam (1907). Fission-track radiography shows uranium to be homogeneously dispersed throughout the opal structure, suggesting coprecipitation of dissolved uranium and silica gel. Fluid inclusions preserved within opal replacements of diatomite have homogenization temperatures in the epithermal range and are of low salinity. Four samples of opal from one locality all have U-Pb apparent ages which suggest uraniferous opal precipitation in late Pliocene time. These ages correspond to a period of local, normal faulting, and highangle faults may have served as vertical conduits for transport of deep, thermalized ground water to shallower levels. Lateral migration of rising solutions occurred at intersections of faults with permeable strata. Silica and some uranium were dissolved from silica-rich host strata of 5–20 ppm original uranium content and reprecipitated as the solutions cooled. The model predicts that in similar geologic settings, ore-grade concentrations of uranium will occur in permeable strata that intersect high-angle faults and that contain uranium source rocks as well as efficient reductant traps for uranium. In the absence of sufficient quantities of reductant materials, uranium will be flushed from the system or will accumulate in low-grade disseminated hosts such as uraniferous opal.

Nevada↗
USGS1982

Comparison of hot hydroxylamine hydrochloride and oxalic acid leaching of stream sediment and coated rock samples as anomaly enhancement techniques

A hot hydroxylamine hydrochloride (H-Hxl) extraction in 25% acetic acid is compared with the commonly used oxalic acid extraction as a method of anomaly enhancement for Cu and Zn in samples from two very different metal deposits and climatic environments. Results obtained on minus-80-mesh stream sediments from an area near the Magruder massive sulfide deposit in Lincoln County, Georgia, where the climate is humid subtropical, indicate that H-Hxl enhances the anomaly for Cu by a factor of 2 and for Zn by a factor of 1.5, compared to the oxalic method. Analyses of Fe oxide-coated rock samples from outcrops overlying the North Silver Bell porphyry copper deposit near Tucson, Arizona, where the climate is semi-arid to arid, indicate that both techniques effectively outline the zones of hydrothermal alteration. The H-Hxl extraction can also perform well in high-carbonate or high-clay environments, where other workers have suggested that oxalic acid is not very effective. Therefore, the H-Hxl method is recommended for general exploration use.

Journal of Geochemical Exploration↗
USGS1982

Guidelines for finding concretionary Mn-Fe oxides in streams

Concretionary Mn-Fe oxides in streams form at interfaces between oxidizing and reducing environments. A reducing environment produces waters high in dissolved Mn and Fe, and an oxidizing environment causes precipitation. Mineralogical, microprobe, and optical studies of concretionary Mn-Fe oxides may further our understanding of the role of Mn-Fe oxides in determining the trace-element geochemistry of stream sediments.

Journal of Geochemical Exploration↗
USGS1983

The use of sagebrush (Artemisia) as a biogeochemical indicator of base-metal deposits in Precambrian rocks of west-central Colorado

The efficacy of sagebrush ( Artemisia ) as a biogeochemical indicator of base-metal mineralization in stratabound Precambrian ore deposits in west-central Colorado was investigated by collecting new (mostly flowering) growth from several sagebrush shrubs over and near five such deposits in three different areas. These are the Sedalia mine and two mines in the Turret district near Salida, and two mines in the Cochetopa district southeast of Gunnison. Two species were used, A. tridentata and A. frigida , depending on the area. Sagebrush clippings were separated into two subsamples consisting of (1) stems, and (2) leaves and blossoms stripped from the stems. These subsamples were ashed separately and the ash analyzed with an emission spectrograph for 30 elements. There appear to be no appreciable differences in the analyses of the two subsamples, indicating that composite samples would provide adequate information for further investigations. Eight of these elements, Ag, Bi, Cu, Pb, Sn, Y, Zn, and Zr, are present in notably higher concentrations in the ash of samples growing over mineralized ground than in that of control samples growing over barren ground. Although the distribution pattern, and the number of these anomalous elements, differs at each of the five localities, three of them, silver, copper, and lead, show good contrast and close association with subjacent mineralization in all five study areas.

Journal of Geochemical Exploration↗
USGS1984

Copper and cobalt in aquatic mosses and stream sediments from the Idaho Cobalt Belt

Samples of stream sediments and aquatic mosses were collected from nine sites across several mineralized zones at the southeasternmost extension of the Idaho Cobalt Belt. Because the steepness of the terrain and the attendant high flow rate of the streams made it difficult to obtain adequate sediment samples, mosses were considered as an alternative sampling medium. The results not only showed that the Cu and Co content of the mosses correlated almost perfectly with that of the sediments, but that the contrast between samples taken from mineralized and background areas was greater in mosses, especially for Co. Maximum concentrations of 35,000 μg/g Cu and 2000 μg/g Co were observed in the ash of mosses, compared to maximum concentrations of 1700 μg/g and 320 μg/g, respectively, in the associated sediments. Species identification was considered unimportant, which should dispel some reluctance to use mosses in mineral exploration.

Journal of Geochemical Exploration↗
USGS1985

The copper-nickel concentration log: A tool for stratigraphic interpretation within the ultramafic and basal zones of the stillwater complex, Montana

An analogue to the electric well log was devised for copper-nickel concentration drill-hole data from the Basal and lower part of the Ultramafic zones of the Stillwater Complex using automated data processing. The copper-nickel concentration logs graphically represent intensity (concentration) values that reflect the distribution of the elements in sulfide and silicate minerals. Four major patterns are recognized by their characteristic variations in copper and nickel intensity: (1) relatively flat, low-level copper-intensity signatures associated with arcuate nickel-intensity patterns that correlate with rocks in the Peridotite member of the Ultramafic zone; (2) arcuate or bulb-like patterns of copper and nickel intensity that correlate closely with the Basal bronzite cumulate member of the Basal zone; (3) complex patterns consisting of intervals of low-intensity copper and moderate-intensity nickel, spikes of high nickel and copper intensity, and high copper intensity associated with low nickel intensity that correlate respectively with cordierite-pyroxene hornfels, massive sulfide, norites and mineralized diabase dikes in the Basal norite member; and (4) large intervals of extremely low copper and nickel intensity that correlate with quartz-orthopyroxene hornfels. The recognition and interpretation of these patterns allow two- and three-dimensional stratigraphic and lithologic reconstructions to be done by means of concentration-log correlations instead of variable quality lithologic logging.

Journal of Geochemical Exploration↗
USGS1985

Correlations among hydrocarbon microseepage, soil chemistry, and uptake of micronutrients by plants, Bell Creek oil field, Montana

Chelate-extractable iron and manganese concentrations in soils over and around the Bell Creek oil field suggest that compared to low average background values, there are moderate amounts of these elements directly over the production area and higher concentrations distributed in an aureole pattern around the periphery of the field. Adsorbed and organically bound iron and manganese appear to be readily taken up by plants resulting in anomalously high levels of these elements in leaves and needles over the oil field and suggesting correlation with corresponding low concentrations in soils. Iron and manganese appear to have bypassed the soil formation process where, under normal oxidizing conditions, they would have ultimately precipitated as insoluble oxides and hydroxides.

Journal of Geochemical Exploration↗
USGS1986

A tubular-coring device for use in biogeochemical sampling of succulent and pulpy plants

A hand-operated, tubular-coring device developed for use in biogeochemical sampling of succulent and pulpy plants is described. The sampler weighs about 500 g (1.1 lb); and if 25 × 175 mm (1 × 7 in) screw-top test tubes are used as sample containers, the complete sampling equipment kit is easily portable, having both moderate bulk and weight.

Journal of Geochemical Exploration↗
USGS1987

Response of douglas fir (Pseudotsuga menziesii) to uraniferous groundwater in a small glaciated drainage, Northeastern Washington State

Douglas fir trees and associated soils were sampled from the slopes of a small (∼4 km 2 ) drainage basin in northeastern Washington to investigate the biogeochemical response to locally uraniferous groundwater. Uranium is preferentially incorporated in needles and twigs compared to larger branches or the trunk. The U concentration in needle ash ranges from 0.2 to 5.8μg g −1 (ppm) and shows no correlation with the U concentration in associated soils. Rather, the distribution of anomalously uraniferous douglas fir (> 1.0 μ g g −1 U in needle ash) appears to be controlled by observed or readily inferred pathways of near-surface groundwater movement in the drainage. These pathways include: (1) general downslope movement of subsurface runoff; (2) increased flux of near-surface groundwater near the toe of an alluvial fan; and (3) emergence of uraniferous (100–150 ng ml −1 [ppb] groundwater in the vicinity of a slope spring. The data also indicate the presence of near-surface uraniferous groundwater along a structurally controlled zone that parallels the north-south strike of the valley, and that includes the slope spring. The results suggest that biogeochemical sampling may be used to supplement more direct, but more limited, measurements of groundwater quality and flow regime in areas of near-surface contaminated groundwater.

Journal of Geochemical Exploration↗
USGS1988

Concentration of gold in natural waters

The purpose of this paper is to investigate the amount of gold present in natural waters. One hundred and thirty-two natural water samples were collected from various sources and analyzed for gold by the latest techniques. Background values for gold in natural waters range from <0.001 to 0.005 ppb, and anomalous values range from 0.010 to 2.8 ppb. Waters collected from mineralized areas have a mean gold value of 0.101 ppb, whereas waters collected from unmineralized areas have a mean of 0.002 ppb. Some of the high gold values reported in the earlier literature were probably due to interferences by high salt content in the sample and/or lack of proper filter procedures.

Journal of Geochemical Exploration↗
USGS1989

Soil geochemistry of Mother Lode-type gold deposits in the Hodson mining district, central California, U.S.A.

The Hodson mining district is in the westernmost foothills of the Sierra Nevada in California, about 17 km west of the town of Angels Camp. This district is part of the West Gold Belt, which lies about 12-16 km west of, and generally parallel to, the better known Mother Lode Gold Belt in central California. The district produced several million dollars worth of Au between about 1890 and 1940. The geologic setting and mineral deposits in the West Gold Belt are generally similar to those in the Mother Lode Gold Belt. Rocks in the study area are of Jurassic age and consist of a mixture of (1) fine-grained, generally thin-bedded, clastic sedimentary rocks that have been metamorphosed to slates, schists, and phyllites, and (2) massive volcanic flows and welded tuffs that have been metamorphosed to metabasalts and metatuffs. All rocks were intensely faulted and folded during the Late Cretaceous Nevadan orogeny; northnorthwest- and northwest-trending faults dominate. Mining in the area was of low-grade gold-pyrite ores occurring principally in the carbonatized wall rocks adjacent to the major northwest-trending Hodson fault and its splays. Minor amounts of other sulfide minerals (principally chalcopyrite, arsenopyrite, sphalerite, and galena) are locally associated with the Au deposits.

California↗
USGS1990

Geology and geochemistry of epithermal precious metal vein systems in the intra-oceanic arcs of Palau and Yap, western Pacific

The Palau and Yap arcs are part of an intra-oceanic island-arc-trench system which separates the Pacific and Philippine plates in the western Pacific Ocean. The 350-km-long Palau arc consists of over 200 islands while the 400-km-long Yap arc located to the north has only four major islands exposed. Four of the largest islands in Palau are composed primarily of early Eocene to mid-Miocene volcanic rocks and the four islands comprising Yap contain only Miocene volcanic rocks. Basalt and basaltic andesites of the Babelthuap Formation are the oldest volcanic rocks in Palau and are characterized by high MgO, Ni and Cr and low TiO 2 and have a boninitic affinity. They form the central and southeastern parts of Babelthuap Island. Oligocene arc tholeiite flows having an age of 34–35.5 Ma comprise most of the three smaller volcanic islands in Palau and the western part of Babelthuap. The youngest volcanic rocks are dacitic intrusions having an age of 22.7–23.2 Ma. The Yap arc is unusual in that metamorphic rocks up to amphibolite grade form most of the islands. These are underlain by a melange composed of igneous and volcanic clasts as well as clasts from a dismembered copper-gold skarn deposit. Miocene volcanic rocks consisting of flows and volcaniclastic deposits overlie the melange and metamorphic complex.

Journal of Geochemical Exploration↗
USGS1990

Platinum-group element abundance and distribution in chromite deposits of the Acoje Block, Zambales Ophiolite Complex, Philippines

Platinum-group elements (PGE) occur in ore-grade concentration in some of the chromite deposits related to the ultramafic section of the Acoje Block of the Zambales Ophiolite Complex. The deposits are of three types: Type 1 - associated with cumulate peridotites at the base of the crust; Type 2 - in dunite pods from the top 1 km of mantle harzburgite; and Type 3 - like Type 2, but in deeper levels of the harzburgite. Most of the deposites have chromite compositions that are high in Cr with Cr/(Cr + Al) (expressed as chromium index, Cr#) > 0.6; high-Al (Cr# < 0.6) chromite deposits are relatively rare, occurring as interspersed orebodies in regions of Types 2 and 3. Sulfide-bearing Type 1 high-Cr deposits are PGE-enriched; the high-Al deposits have lowest Ir and Pd. Among the PGEs, Ir ranges from <20 to 550 ppb, Rh from <100 to 1100 ppb, Rh from 0.7 to 760 ppb, Pt from <1.0 to 5960 ppb and Pd from <0.5 to 8350 ppb. Chondrite-normalized (CN) PGE patterns are diverse, and include those with both negative slope (Ir > Pd, thought to be characteristic of PGE-barren deposits) and positive slope (Ir < Pd, characteristic of PGE-rich deposits). Iridium, Ru and Os commonly occur as micron-size laurite (sulfide) inclusions in unfractured chromite. Laurite and native Os are also found as inclusions in interstitial sulfides. Platinum and Pd occur as alloy inclusions (and possibly as solid solution) in interstitial Ni-Cu sulfides and as tellurobismuthides in serpentine and altered sulfides.

Journal of Geochemical Exploration↗
USGS1990

Production of sulfur gases and carbon dioxide by synthetic weathering of crushed drill cores from the Santa Cruz porphyry copper deposit near Casa Grande, Pinal County, Arizona

Samples of ground drill cores from the southern part of the Santa Cruz porphyry copper deposit, Casa Grande, Arizona, were oxidized in simulated weathering experiments. The samples were also separated into various mineral fractions and analyzed for contents of metals and sulfide minerals. The principal sulfide mineral present was pyrite. Gases produced in the weathering experiments were measured by gas chromatography. Carbon dioxide, oxygen, carbonyl sulfide, sulfur dioxide and carbon disulfide were found in the gases; no hydrogen sulfide, organic sulfides, or mercaptans were detected. Oxygen concentration was very important for production of the volatiles measured; in general, oxygen concentration was more important to gas production than were metallic element content, sulfide mineral content, or mineral fraction (oxide or sulfide) of the sample. The various volatile species also appeared to be interactive; some of the volatiles measured may have been formed through gas reactions.

Journal of Geochemical Exploration↗